Sodium bis(trimethylsilyl)amide → HCID 135563255, compound

Temperature

-78 °C

To a cold (-78° C.) solution of N-propargylbenzamidine (5.50 g, 34.77 mmol) in 150 mL of THF was added sodium bis(trimethylsilyl)amide (36.51 mL, 36.51 mmol, 1.05 equiv, 1M solution in THF) over 20 minutes. The reaction mixture was stirred for 5 minutes at -78° C., followed by the addition of a cold (-78° C.) solution of ethylmalonyl dichloride (6.46 g, 38.25 mmol, 1.1 equiv.) in 150 mL of THF via a canula over 2 hours. After stirring for 30 minutes, the reaction mixture was quenched with 100 mL of water, warmed to room temperature, and diluted with 300 mL of ethyl acetate and 100 mL of water. The organic layer was successively washed with 200 mL of water and 200 mL of saturated sodium chloride, dried (MgSO4), filtered, and concentrated to give a solid. The crude mixture was azeotropically evaporated with 200 mL of toluene to remove residual hexamethyldisilazane, affording 8.28 g of 5-ethyl-6-hydroxy-2-phenyl-3-propargyl-4(3H)-pyrimidinone which was used without further purification.

1. stirringAfter stirring for 30 minutes
2. customthe reaction mixture was quenched with 100 mL of water
3. temperaturewarmed to room temperature
4. additiondiluted with 300 mL of ethyl acetate and 100 mL of water
5. washThe organic layer was successively washed with 200 mL of water and 200 mL of saturated sodium chloride
6. dry with materialdried (MgSO4)
7. filtrationfiltered
8. concentrationconcentrated
9. customto give a solid
10. customThe crude mixture was azeotropically evaporated with 200 mL of toluene
11. customto remove residual hexamethyldisilazane

ORD record

ord-5afb9843d09540d984b827ca765bf208

Source dataset

uspto-grants-2000_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06051710